Our purpose was to identify and localize intrinsic cardiac ganglia innervating distinct regions of the heart using postmortem tracing of nerve projections with DiI, a method not previously used to study the intrinsic cardiac nervous system. We also investigated the possibility of collateral innervation of myocardium and intrinsic ganglia. In isolated paraformaldehyde-fixed guinea pig hearts, crystals of DiI (1,1′- dioctadecyl-3,3,3′,3′-tetramethylin-docarbocyanine perchlorate) were inserted into the posterior ventricular myocardium below the atrioventricular groove, the right atrium, or the left ventricular septum. Hearts were placed in the dark at 37°C for 2-14 weeks to allow DiI diffusion within neuronal membranes. Labeled neurons were observed in intracardiac ganglia after at least 4 weeks of dye exposure. Labeling was restricted to the inferior-most ganglia (those near the atrioventricular groove) when DiI was inserted into the posterior ventricular myocardium and to ganglia near the sinus node after right atrial DiI placement. Application of DiI to the left ventricular septum resulted in neuron labeling in ganglia primarily in the interatrial septum near the atrioventricular node. After 8 weeks, DiI-labeled nerve fibers and varicosities were seen surrounding unlabeled neurons in some ganglia, suggesting that axons terminating in or passing through the DiI application site in posterior ventricular tissue had collateral branches innervating these ganglia. These results indicate that intrinsic innervation of major cardiac subdivisions is accomplished by regionally segregated cardiac ganglia. Also, tracing with DiI has provided evidence for collateral nerve projections that could be the substrate for novel intracardiac regulatory circuits.

Thesis advisor: Elizabeth Kensinger / Individuals with social anxiety disorder (SAD) tend to have emotional memory biases in the encoding and retrieval of social memories. Research has shown reduced heart rate variability (HRV) in clinical populations suffering from anxiety, including social anxiety. Heightened sympathetic activation—as measured by the electrodermal activity (EDA)—has also been associated with anxiety disorders. The aim of the present study was to examine the relation between HRV, social anxiety, and re-experiencing of emotional autobiographical memories. 44 healthy young adults were recruited from the Boston College campus through SONA. Participants were given an online survey that instructed them to retrieve 40 specific events from the past in response to 40 socially relevant cues. For each event, participants were instructed to provide a brief narrative, make several ratings for the event (on a scale from 1-7), and indicate the specific emotions they experienced both at the time of retrieval and of the event. Approximately one month after the completion of the memory survey, participants engaged in a 2-hour memory retrieval session while undergoing psychophysiological monitoring (heart rate, skin conductance, and respiration). Following the retrieval task, participants completed self-report questionnaires of social anxiety symptom severity and trait emotion regulation strategy (i.e., tendency to reappraise or suppress emotions). The present study found that positive memories had higher re-experiencing ratings as compared to negative memories. Contrary to the original study hypothesis, however, there was no significant interaction between average re-experiencing (or arousal) ratings of positive or negative social autobiographical memories and SAD likelihood. A nonlinear, cubic relationship was found between one of three metrics of HRV and social anxiety symptom severity. A significant effect was found between skin conductance and SAD likelihood, which was likely driven by an almost significance difference in skin conductance between the SAD unlikely and the SAD very probable groups; these findings provide further insight into the relationship between autonomic nervous system (ANS) functioning and social anxiety. Further, the present results suggest the intriguing possibility that there may be a nonlinear relationship between HRV and severity of social anxiety. Future research with a larger sample size is needed to corroborate these findings. / Thesis (BS) — Boston College, 2018. / Submitted to: Boston College. College of Arts and Sciences. / Discipline: Departmental Honors. / Discipline: Psychology.

The origin of cardiac preganglionic neurons in the rat was investigated using the retrograde transport of horseradish peroxidase (HRP). A single injection of HRP was made into the right myocardium in either a sinoatrial or mid-ventricular location. Labeled cells were found in the mid- and lower medulla primarily in and around the nucleus ambiguus (NA) 600-1800 μm above the obex. The dorsal motor nucleus of X (DMN) was sparsely labeled and a few cells were found in an intermediate zone near the level of the obex. Labeling was bilateral with slightly heavier labeling found ipsilateral to the injection site than contralateral to it. Following a unilateral vagotomy, labeled cells were only found ipsilateral to the intact vagus. Atrial and midventricular injections yielded similar results. Occasionally only 1- cells in the NA were labeled per section. Inspection of serial sections revealed that in these sparsely labeled rats, the HRP was often in the same location within the NA forming a column of cells within the nucleus. The columns sometimes extended at least 240 μm in the rostral-caudal direction. The columnar organization was most apparent in rats with few labeled cells presumably because it was obscured in nuclei that were heavily labeled. In a second group of rats, the right vagus was cut at the cervical level and dipped in HRP to determine the extent of the NA and DMN in rats. In these animals, heavier labeling was found in the DMN than in the NA. Cells in the DMN were filled from the upper spinal cord to its most rostral extent 1200 μm above the obex. Thus, although the DMN and NA send projections in the vagus nerve, those axons terminating in the myocardium primarily originate in the NA.

Traumatic damage to the cervical spinal cord has a dramatic impact on determinants affecting cardiovascular fitness. In tetraplegia, in addition to diminished skeletal muscle function, impaired sympathetic cardiovascular innervation together with a dysfunction of catecholamine release is typically present. Individuals with tetraplegia are at a high risk of long-term inactivity, which increasingly contributes to the development of common civilization diseases. The aim of the current dissertation project is to investigate the cardiovascular fitness in males with cervical spinal cord injury (n=20) as compared to able- bodied males (n=27). Both groups completed exercise testing on an arm-crank ergometer. Arterial blood pressure response to exercise, peak oxygen consumption and peak heart rate were the primary outcome variables. In the first part of the study, a graded maximal arm- crank ergometer test to the subjective exhaustion was performed for the inter-group peak exercise comparison. The peak power dramatically differs between the groups and could be an important confounding factor limiting the evaluation of a physiologic response related to the equivalent physical loading. Therefore, in the second part of the study, individuals of the control group completed a second graded arm-crank ergometer...

Murine models have become increasingly popular to study various aspects of cardiovascular diseases due to their ease of genetic manipulation. Unfortunately, there has been little effort put into describing the distribution of autonomic nerves in the mouse heart, making it difficult to compare current findings from clinical and experimental models related to cardiovascular diseases. Furthermore, determination of the requirements for the development of this system and its maintenance in adult mice remains largely unexplored. This study represents the first detailed mapping of cholinergic neuroanatomy of the mouse heart based on immunohistochemical staining using true cholinergic markers. We found cholinergic innervation of the mouse heart to be largely focused in the atrium and conducting system. We investigated the involvement of the neurotrophic factor neurturin (NRTN) in the development of cholinergic innervation, because there was indirect evidence that implicated it as a crucial factor. Results from our work definitively demonstrate that NRTN plays a major role in the development of cardiac parasympathetic ganglia and cholinergic innervation of the mouse heart. Adult NRTN knockout mice exhibited a drastic reduction in the number of intracardiac neurons with decreased atrial acetylcholine, cholinergic nerve density at the sinoatrial node and negative chronotropic responses to vagal stimulation. The presence of NRTN and its receptors in hearts from adult wild-type mice suggests that this neurotrophic factor might also be required for maintenance of cardiac cholinergic innervation. Finally, we wanted to determine how intracardiac neurons and their processes change during diseased states, specifically type 1 diabetes. This work has shown that the cardiac cholinergic nervous system in the mouse undergoes structural and functional remodeling when challenged with streptozotocin-induced diabetes. Cholinergic nerves in diabetic hearts undergo extensive sprouting at the sinoatrial node with no change in the number of intracardiac neurons. Cholinergic function appears to be enhanced in diabetic mice, based on pharmacological testing, despite decreased response to direct vagal nerve stimulation. Evidence also suggests that diabetic mice have an imbalance in autonomic control of heart rate. The latter findings suggest that disruption of central input into intrinsic cardiac ganglia also contributes to the neuropathology of type 1 diabetes.

No description available.

Gross' emotion regulation model, Porges' polyvagal theory, and other existing research suggest that regulation of emotions, tactics used to handle conflict, and certain physiological processes that occur within the autonomic nervous system (ANS) in response to stress are significantly related, especially in relational contexts. However, despite their pervasiveness and negative impacts, there is a noticeable lack of research on predictors of violent, aggressive, or abusive conflict tactics in couples. In the current study, the predictive role of emotion regulation in relation to conflict tactics was examined, in addition to the role of respiratory sinus arrhythmia (RSA) and pre-ejection period (PEP) as mediators for these variables. Thirty-eight participants (19 couples) completed self-report measures of emotion regulation and conflict tactics, and RSA and PEP were measured during a three-minute baseline and 20-minute conflict discussion. Results showed no significant relationships between emotion regulation and conflict tactics, and no significant relationships between these variables and RSA or PEP were found. These findings may suggest that other variables aside from measures of ANS activity better explain the relationship between emotional and behavioral regulation skills, though additional research is necessary to confirm these findings. Clinical implications of this research point to the exploration of other contributors to violence and aggression aside from poor emotion regulation as it was measured in this study. Future research may benefit from investigating the impact of other variables such as sleep and exercise on ANS reactivity in relation to the use of maladaptive conflict tactics in married couples.

Sympathovagal imbalance is known to precede the on-set of atrial fibrillation (AF) and has been analyzed extensively based on heart rate variability (HRV). However, the relationship between sympathetic and vagal effects before AF onset and their influence on various HRV features have not been fully elucidated. QT interval variability (QTV) reflects sympathetic activity and may therefore provide further insights into this relationship. Using the time delay stability (TDS) method, we investigated temporal changes in coupling behavior before AF onset between 20 vagal or sympathovagal-associated HRV and QTV features. We applied the TDS method to 26 electrocardiograms from the MIT-BIH AF database with at least one hour of sinus rhythm preceding AF onset. Sinus rhythm segments were split into 5-minute windows with 50 % overlap. Logistic regression analysis revealed significantly (p<0.01) increased coupling between QTV and vagal HRV features from 20 to 15 minutes before AF onset. We found similar behavior between QTV and sympathovagal HRV features. This indicates sympathetic predominance increasing until 15 minutes before the onset of AF and decreasing towards vagal predominance right before AF onset. Our results provide new insights into temporal changes of sympathovagal imbalance preceding AF onset and may improve the prediction of AF in clinical applications.

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No description available.